Evidence map›Paper›PMID 30998783›Full record

ArticlePLoS pathogens2019

Distinct phenotype and function of circulating Vδ1+ and Vδ2+ γδT-cells in acute and chronic hepatitis B.

Kyong-Mi Chang, Daniel Traum, Jang-June Park, Suzanne Ho, Keisuke Ojiro, David K Wong, Abdus S Wahed, Norah A Terrault, Mandana Khalili, Richard K Sterling and 10 more

Abstract read
In one paragraph

Article in PLoS pathogens, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

22 citing papers in PubMed.

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  16. Murine CXCR3Frontiers in immunology · 2021
    Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors.

Kyong-Mi ChangMedical Research, The Corporal Michael J. Crescenz VA Medical Center, Philadelphia PA, United States of America.ORCID 0000-0001-6811-9364
Daniel TraumMedical Research, The Corporal Michael J. Crescenz VA Medical Center, Philadelphia PA, United States of America.ORCID 0000-0002-0195-5525
Jang-June ParkMedical Research, The Corporal Michael J. Crescenz VA Medical Center, Philadelphia PA, United States of America.
Suzanne HoMedical Research, The Corporal Michael J. Crescenz VA Medical Center, Philadelphia PA, United States of America.
Keisuke OjiroMedical Research, The Corporal Michael J. Crescenz VA Medical Center, Philadelphia PA, United States of America.
David K WongToronto Centre for Liver Disease, University of Toronto, Toronto, Ontario, Canada.ORCID 0000-0002-3310-3538
Abdus S WahedUniversity of Pittsburgh Graduate School of Public Health, Pittsburgh PA, United States of America.
Norah A TerraultDepartment of Medicine, University of California, San Francisco, San Francisco CA, United States of America.
Mandana KhaliliDepartment of Medicine, University of California, San Francisco, San Francisco CA, United States of America.ORCID 0000-0001-9178-9139
Richard K SterlingDepartment of Internal Medicine, Virginia Commonwealth University, Richmond VA, United States of America.
Harry L A JanssenToronto Centre for Liver Disease, University of Toronto, Toronto, Ontario, Canada.
Margaret C ShuhartHarborview Medical Center, University of Washington Medical Center, Seattle WA, United States of America.
Daryl T LauDepartment of Medicine, Beth Israel Deaconess Medical Center, Boston MA, United States of America.
Lewis R RobertsDepartment of Internal Medicine, Mayo Clinic, Rochester MN, United States of America.ORCID 0000-0001-7885-8574
Geoffrey S JohnsonUniversity of Pittsburgh Graduate School of Public Health, Pittsburgh PA, United States of America.ORCID 0000-0001-7931-494X
David E KaplanMedical Research, The Corporal Michael J. Crescenz VA Medical Center, Philadelphia PA, United States of America.
Michael R BettsDepartment of Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia PA, United States of America.
William M LeeDepartment of Internal Medicine, University of Texas Southwestern Medical Center, Dallas TX, United States of America.
Anna S F LokDepartment of Internal Medicine, University of Michigan, Ann Arbor MI, United States of America.
Hepatitis B Research Network (HBRN)

Funding

Engaging University of California Stakeholders for Biorespository ResearchUL1TR000004 · NCATS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GRANDIS, JENNIFER RUBIN · 2012 to 2015
$78.0M
North Carolina Translational & Clinical Sciences Institute (NC TraCS)UL1TR001111 · NCATS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BUSE, JOHN BERNARD, CAREY, TIMOTHY S · 2013 to 2017
$43.9M
TRANSGENIC AND CHIMERIC MOUSE COREP30DK050306 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI REBECCA G WELLS · 1997 to 2026
$32.5M
Hepatitis B Research Network - Data Coordination CenterU01DK082864 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI BELLE, STEVEN H. · 2008 to 2019
$25.3M
ZDV VS ZDV + DDL VS ZDV + DDL + NVP IN ASYMPTOMATIC HIV PATIENTSM01RR000040 · NCRR · UNIVERSITY OF PENNSYLVANIA · PI FITZGERALD, GARRET A · 1985 to 2006
$21.1M
Center for Clinical and Translational ResearchUL1TR000058 · NCATS · VIRGINIA COMMONWEALTH UNIVERSITY · PI MOELLER, FREDERICK GERARD · 2012 to 2015
$12.5M
Hepatitis B Research Network (HBRN): Natural History and Treatment StudiesU01DK082944 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI COOPER, STEWART, KHALILI, MANDANA · 2008 to 2019
$10.0M
Observation Study of Persons with Chronic Hepatitis B Virus infection in North AmericaU01DK082874 · NIDDK · UNIVERSITY HEALTH NETWORK · PI JANSSEN, HARRY · 2008 to 2019
$6.9M
Harvard Hepatitis B ConsortiumU01DK082919 · NIDDK · BETH ISRAEL DEACONESS MEDICAL CENTER · PI CHUNG, RAYMOND T, LAU, DARYL T · 2008 to 2019
$4.7M
Midwest Hepatitis B ConsortiumU01DK082871 · NIDDK · SAINT LOUIS UNIVERSITY · PI DI BISCEGLIE, ADRIAN MICHAEL · 2008 to 2019
$4.7M
Hepatitis B Clinical Research Network Clinical Center: Michigan - Hawaii ConsortiumU01DK082863 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LOK, ANNA S.F. · 2008 to 2020
$3.7M
The North Carolina Hepatitis Beta Clinical Research NetworkU01DK082867 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI FRIED, MICHAEL W · 2008 to 2019
$3.4M
BLRD VA I01 BX000649NCATS NIH HHS UL1 TR000004NCATS NIH HHS UL1 TR000058NCATS NIH HHS UL1 TR001111NCRR NIH HHS M01 RR000040NIAAA NIH HHS K24 AA022523NIAID NIH HHS R01 AI047519NIDDK NIH HHS P30 DK050306NIDDK NIH HHS U01 DK082843NIDDK NIH HHS U01 DK082863NIDDK NIH HHS U01 DK082864NIDDK NIH HHS U01 DK082866NIDDK NIH HHS U01 DK082867NIDDK NIH HHS U01 DK082871NIDDK NIH HHS U01 DK082872NIDDK NIH HHS U01 DK082874NIDDK NIH HHS U01 DK082919NIDDK NIH HHS U01 DK082923NIDDK NIH HHS U01 DK082927NIDDK NIH HHS U01 DK082943NIDDK NIH HHS U01 DK082944
6 · The paper itself

Abstract

Hepatitis B virus (HBV) persists with global and virus-specific T-cell dysfunction, without T-cell based correlates of outcomes. To determine if γδT-cells are altered in HBV infection relative to clinical status, we examined the frequency, phenotype and function of peripheral blood Vδ1+ and Vδ2+γδT-cells by multi-parameter cytometry in a clinically diverse North American cohort of chronic hepatitis B (CHB), acute hepatitis B (AHB) and uninfected control subjects. We show that circulating γδT-cells were comprised predominantly of CD3hiCD4- Vδ2+γδT-cells with frequencies that were 2-3 fold higher among Asian than non-Asian Americans and inversely correlated with age, but without differences between CHB, AHB and control subjects. However, compared to control subjects, CHB was associated with increased TbethiEomesdim phenotype in Vδ2+γδT-cells whereas AHB was associated with increased TbethiEomesdim phenotype in Vδ1+γδT-cells, with significant correlations between Tbet/Eomes expression in γδT-cells with their expression of NK and T-cell activation and regulatory markers. As for effector functions, IFNγ/TNF responses to phosphoantigens or PMA/Ionomycin in Vδ2+γδT-cells were weaker in AHB but preserved in CHB, without significant differences for Vδ1+γδT-cells. Furthermore, early IFNγ/TNF responses in Vδ2+ γδT-cells to brief PMA/Ionomycin stimulation correlated inversely with serum ALT but not HBV DNA. Accordingly, IFNγ/TNF responses in Vδ2+γδT-cells were weaker in patients with CHB with hepatitis flare compared to those without hepatitis flares, and this functional deficit persisted beyond clinical resolution of CHB flare. We conclude that circulating γδT-cells show distinct activation and differentiatiation in acute and chronic HBV infection as part of lymphoid stress surveillance with potential role in clinical outcomes.

Indexed as

AdolescentAdultAgedBiomarkersCohort StudiesFemaleHepatitis B, ChronicHepatitis B virusHumansLymphocyte ActivationMaleMiddle AgedPhenotypeReceptors, Antigen, T-Cell, gamma-deltaT-LymphocytesYoung AdultBiomarkersReceptors, Antigen, T-Cell, gamma-delta

Identifiers

PMID30998783
PMCPMC6490945

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.